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H Giles

Showing results (471-480 of 503) with videos related to

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Ethnicity & Disease|July 29, 1998
Thermolabile methylenetetrahydrofolate reductase polymorphism (C677T) and total homocysteine concentration among African-American and white womenW H Giles, S J Kittner, C Y Ou, et al.
Oncogene|February 2, 1999
Genomic acute myeloid leukemia-associated inv(16)(p13q22) breakpoints are tightly clusteredB A van der Reijden, H G Dauwerse, R H Giles, et al.
Human Molecular Genetics|November 3, 2018
Loss-of-function mutations in KIF14 cause severe microcephaly and kidney development defects in humans and zebrafishMadeline Louise Reilly, Marijn F Stokman, Virginie Magry, et al.
Experimental & Molecular Medicine|July 1, 2018
Targeted deletion of the AAA-ATPase Ruvbl1 in mice disrupts ciliary integrity and causes renal disease and hydrocephalusClaudia Dafinger, Markus M Rinschen, Lori Borgal, et al.
Nature Communications|December 20, 2025
SETD1A regulates psychiatric gene networks involved in genomic stability and synaptic function in rare and sporadic schizophreniaTomoyo Sawada, Arthur S Feltrin, Yanhong Wang, et al.
Human Molecular Genetics|June 21, 2013
Birt-Hogg-Dube syndrome is a novel ciliopathyMonique N H Luijten, Sander G Basten, Tijs Claessens, et al.
Human Mutation|April 27, 2022
Large scale genotype- and phenotype-driven machine learning in Von Hippel-Lindau diseaseAndreea Chiorean, Kirsten M Farncombe, Sean Delong, et al.
Cancer|May 17, 2022
Multidisciplinary integrated care pathway for von Hippel-Lindau diseaseWendy P G Wolters, Koen M A Dreijerink, Rachel H Giles, et al.
Stroke|March 20, 1998
Platelet glycoprotein receptor IIIa polymorphism P1A2 and ischemic stroke risk: the Stroke Prevention in Young Women StudyK R Wagner, W H Giles, C J Johnson, et al.
European Journal of Human Genetics : EJHG|August 18, 2016
Compound heterozygous NEK1 variants in two siblings with oral-facial-digital syndrome type II (Mohr syndrome)Glen R Monroe, Isabelle Fpm Kappen, Marijn F Stokman, et al.
Pageof 51

Showing results (471-480 of 503) with videos related to

Sort By:
Pageof 51
Ethnicity & Disease|July 29, 1998
Thermolabile methylenetetrahydrofolate reductase polymorphism (C677T) and total homocysteine concentration among African-American and white womenW H Giles, S J Kittner, C Y Ou, et al.
Oncogene|February 2, 1999
Genomic acute myeloid leukemia-associated inv(16)(p13q22) breakpoints are tightly clusteredB A van der Reijden, H G Dauwerse, R H Giles, et al.
Human Molecular Genetics|November 3, 2018
Loss-of-function mutations in KIF14 cause severe microcephaly and kidney development defects in humans and zebrafishMadeline Louise Reilly, Marijn F Stokman, Virginie Magry, et al.
Experimental & Molecular Medicine|July 1, 2018
Targeted deletion of the AAA-ATPase Ruvbl1 in mice disrupts ciliary integrity and causes renal disease and hydrocephalusClaudia Dafinger, Markus M Rinschen, Lori Borgal, et al.
Nature Communications|December 20, 2025
SETD1A regulates psychiatric gene networks involved in genomic stability and synaptic function in rare and sporadic schizophreniaTomoyo Sawada, Arthur S Feltrin, Yanhong Wang, et al.
Human Molecular Genetics|June 21, 2013
Birt-Hogg-Dube syndrome is a novel ciliopathyMonique N H Luijten, Sander G Basten, Tijs Claessens, et al.
Human Mutation|April 27, 2022
Large scale genotype- and phenotype-driven machine learning in Von Hippel-Lindau diseaseAndreea Chiorean, Kirsten M Farncombe, Sean Delong, et al.
Cancer|May 17, 2022
Multidisciplinary integrated care pathway for von Hippel-Lindau diseaseWendy P G Wolters, Koen M A Dreijerink, Rachel H Giles, et al.
Stroke|March 20, 1998
Platelet glycoprotein receptor IIIa polymorphism P1A2 and ischemic stroke risk: the Stroke Prevention in Young Women StudyK R Wagner, W H Giles, C J Johnson, et al.
European Journal of Human Genetics : EJHG|August 18, 2016
Compound heterozygous NEK1 variants in two siblings with oral-facial-digital syndrome type II (Mohr syndrome)Glen R Monroe, Isabelle Fpm Kappen, Marijn F Stokman, et al.
Pageof 51